Canonical Allele Identifier: CA169325

Gene: RAD51D

Linked Data

• ClinVar Variation Id: 142754
• ClinVar RCV Id: RCV000132135 ; RCV000464954 ; RCV001566788
• dbSNP Id: rs587782695
• MyVariant Identifiers: chr17:g.33433434G>A (hg19) ; chr17:g.35106415G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35106415G>A , CM000679.2:g.35106415G>A	GRCh38
NC_000017.10:g.33433434G>A , CM000679.1:g.33433434G>A	GRCh37
NC_000017.9:g.30457547G>A	NCBI36
NG_031858.1:g.18455C>T , LRG_516:g.18455C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.412C>T	ENSP00000468273.3:p.Gln138Ter
ENST00000587405.6:c.190C>T	ENSP00000466478.2:p.Gln64Ter
ENST00000590016.6:c.607C>T	ENSP00000466399.1:p.Gln203Ter
ENST00000590631.2:n.503C>T
ENST00000592577.6:c.190C>T	ENSP00000466839.2:p.Gln64Ter
ENST00000345365.11:c.547C>T MANE Select	ENSP00000338790.6:p.Gln183Ter
ENST00000335858.11:c.211C>T	ENSP00000338408.6:p.Gln71Ter
ENST00000345365.10:c.547C>T	ENSP00000338790.6:p.Gln183Ter
ENST00000394589.8:c.547C>T	ENSP00000378090.4:p.Gln183Ter
ENST00000415064.6:n.697C>T
ENST00000460118.6:c.16C>T	ENSP00000464356.2:p.Gln6Ter
ENST00000585947.5:n.443C>T
ENST00000585982.5:n.567C>T
ENST00000586044.5:c.*278C>T	ENSP00000465584.1:n.*278C>T
ENST00000586210.5:c.*141C>T	ENSP00000465612.1:n.*141C>T
ENST00000587405.5:c.190C>T	ENSP00000466478.1:p.Gln64Ter
ENST00000587977.5:c.*287C>T	ENSP00000466587.1:n.*287C>T
ENST00000587982.5:n.340C>T
ENST00000588372.5:c.190C>T	ENSP00000468764.1:p.Gln64Ter
ENST00000588594.5:c.*143C>T	ENSP00000465366.1:n.*143C>T
ENST00000590016.5:c.607C>T	ENSP00000466399.1:p.Gln203Ter
ENST00000590631.1:c.16C>T	ENSP00000465033.1:p.Gln6Ter
ENST00000591723.5:c.16C>T	ENSP00000467986.1:p.Gln6Ter
ENST00000592181.1:c.190C>T	ENSP00000464799.1:p.Gln64Ter
ENST00000592430.5:n.516C>T
ENST00000592577.5:c.553C>T	ENSP00000466839.1:p.Gln185Ter
ENST00000593039.5:c.70C>T	ENSP00000466834.1:p.Gln24Ter
NM_001142571.1:c.607C>T	NP_001136043.1:p.Gln203Ter
NM_002878.3:c.547C>T , LRG_516t1:c.547C>T	NP_002869.3:p.Gln183Ter
NM_133629.2:c.211C>T	NP_598332.1:p.Gln71Ter
NR_037711.1:n.684C>T
NR_037712.1:n.549C>T
NR_037714.1:n.299C>T
NM_001142571.2:c.607C>T	NP_001136043.1:p.Gln203Ter
NM_133629.3:c.211C>T	NP_598332.1:p.Gln71Ter
NR_037711.2:n.573C>T
NR_037712.2:n.438C>T
NM_002878.4:c.547C>T MANE Select	NP_002869.3:p.Gln183Ter